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Atropine Sulfate - 61314-303-01 - (atropine sulfate)

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Drug Information of Atropine Sulfate

Product NDC: 61314-303
Proprietary Name: Atropine Sulfate
Non Proprietary Name: atropine sulfate
Active Ingredient(s): 1    mg/mL & nbsp;   atropine sulfate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Atropine Sulfate

Product NDC: 61314-303
Labeler Name: FALCON LABORATORY LTD
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000630

Package Information of Atropine Sulfate

Package NDC: 61314-303-01
Package Description: 5 mL in 1 BOTTLE, PLASTIC (61314-303-01)

NDC Information of Atropine Sulfate

NDC Code 61314-303-01
Proprietary Name Atropine Sulfate
Package Description 5 mL in 1 BOTTLE, PLASTIC (61314-303-01)
Product NDC 61314-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name atropine sulfate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20000630
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name FALCON LABORATORY LTD
Substance Name ATROPINE SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Atropine Sulfate


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